Canonical Allele Identifier: CA2362531927

Gene: SRC

Linked Data

• dbSNP Id: rs2070589700
• gnomAD v4: 20-37393657-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37393657G>A , CM000682.2:g.37393657G>A	GRCh38
NC_000020.10:g.36022060G>A , CM000682.1:g.36022060G>A	GRCh37
NC_000020.9:g.35455474G>A	NCBI36
NG_023033.1:g.53973G>A , LRG_1018:g.53973G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358208.9:c.402-238G>A	ENSP00000350941.5:n.402-238G>A
ENST00000692112.1:c.351-238G>A	ENSP00000508666.1:n.351-238G>A
ENST00000692423.1:c.351-238G>A	ENSP00000509325.1:n.351-238G>A
ENST00000373578.7:c.351-238G>A MANE Select	ENSP00000362680.2:n.351-238G>A
ENST00000358208.8:c.351-238G>A	ENSP00000350941.4:n.351-238G>A
ENST00000373558.2:c.369-238G>A	ENSP00000362659.2:n.369-238G>A
ENST00000373567.6:c.351-238G>A	ENSP00000362668.2:n.351-238G>A
ENST00000373578.6:c.351-238G>A	ENSP00000362680.2:n.351-238G>A
ENST00000472968.1:n.182-238G>A
NM_005417.4:c.351-238G>A	NP_005408.1:n.351-238G>A
NM_198291.2:c.351-238G>A , LRG_1018t1:c.351-238G>A	NP_938033.1:n.351-238G>A
XM_011529013.1:c.351-238G>A	XP_011527315.1:n.351-238G>A
XM_011529014.1:c.351-238G>A	XP_011527316.1:n.351-238G>A
XM_011529013.2:c.351-238G>A	XP_011527315.1:n.351-238G>A
XM_017028024.1:c.369-238G>A	XP_016883513.1:n.369-238G>A
XM_017028025.1:c.369-238G>A	XP_016883514.1:n.369-238G>A
XM_017028026.1:c.369-238G>A	XP_016883515.1:n.369-238G>A
XM_017028027.2:c.369-238G>A	XP_016883516.1:n.369-238G>A
NM_005417.5:c.351-238G>A	NP_005408.1:n.351-238G>A
NM_198291.3:c.351-238G>A MANE Select	NP_938033.1:n.351-238G>A